Comparison of an Alginate Containing Enteral Feed and an Alginate Free Enteral Feed.

Enteral Nutrition Clinical Trial

— AlgiNG  

Official title:

Gastric, Biochemical, Endocrine and Appetitive Responses to an Enterally Fed Alginate-containing Feed, Compared With an Alginate Free Feed

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04113200
• Other study ID #: RGS129061
• Status: Completed
• Phase: N/A
• Start date: January 29, 2019
• Est. completion date: March 30, 2020

Study information

• Verified date: September 2022
• Source: University of Nottingham
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

When patients cannot eat and drink enough a tube can be placed through their nostril, down the back of their throat into their stomach and used to give their nutrition as a liquid feed. One of the commonest problems when using this tube is regurgitation of feed up from the stomach (gastro- oesophageal reflux (GOR)), or liquid stools (diarrhoea). This can cause the patient discomfort, a higher risk of getting a skin or chest infection, and increase the risk that the feed is stopped. The investigators intend to investigate, in twelve healthy young men, whether adding a form of dietary fibre (alginate) to the feed could reduce these symptoms (diarrhoea and GOR), hence ensuring patients are properly nourished and recover as quickly as possible from their illness, Each volunteer will come to the lab twice and will have a tube inserted into the stomach via the nose so that they can be given both feeds. Each time, the investigators will take repeated pictures of how the feed is passing through their gut using a non invasive technique called 'magnetic resonance imaging' (MRI), take blood samples to see how quickly the nutrition is absorbed into the blood, and measure how hungry they feel

Description:

TRIAL / STUDY DESIGN Each participant will be required to attend a screening visit, a brief education visit re collecting dietary information, adhering to a standardised diet and faecal sample collection; two, approximately five hour, study visits with 7- 10 days between each visit; and a brief visit after each intervention day to return diet information and the faecal samples. Prior to the study visits they will be required to consume a standardised diet for four days, based on their usual intake with similar macronutrient composition to the feed. On each study visit they will be fed, via a nasogastric enteral tube, 300mls/ hour of one of two enteral feeds (total feed delivered 300mls). The gastric response will be measured using MRI scanning, the biochemical and endocrine response will be measured using arterialised venous blood samples, and the appetitive response will be measured using visual analogue scales, and direct measurement of food intake at an ad libitum test meal. Participants will continue to consume a standardised diet for 3 days after the delivery of the enteral feed. Faecal samples will be collected before and after the visit day, for pH measurement. Ethical approval has been obtained from the Faculty of Medicine and Health Sciences Ethics Committee, University of Nottingham. All participants will provided informed, written consent.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: March 30, 2020
• Est. primary completion date: March 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Non- smoking (non- vaping) males
• aged 18- 45 years
• body mass index (BMI) of 18.5-24.5kg/ m2 or a BMI of 24.5- 26kg/ m2
• a waist circumference of less than 94 cm.
• ability to give informed consent

Exclusion Criteria:

• A history of an acute illness, lasting more than a week, in the last six weeks;
• taking any medications for gastrointestinal disorders, including acid suppressants or anti-spasmodics,
• taking anti-depressants or symptoms of clinical depression (defined by a score >10 on the Beck Depression Inventory)
• taking medication for diabetes or having diabetes
• a history of substance abuse in the last six months;
• having any factors that preclude safe MRI;
• a history of gastrointestinal disorders, including Gastro Oesophgeal Reflux Disease, Irritable Bowel Syndrome, active peptic ulcer disease; having diabetes;
• previous surgery to the gastrointestinal or biliary systems;
• having characteristics of those with an eating disorders (defined by a score of more than 20 on the Eating Attitudes Test (EAT-26));
• having an allergy or intolerance to the ingredients in the enteral feeds, or the cheese and tomato pasta meal

Related Conditions & MeSH terms

• Enteral Nutrition

Intervention

Dietary Supplement:
• MerMed One
A 1 kcal per ml enteral feed containing an alginate.
• Nutricomp Soy Fibre
A 1kcal per ml enteral feed not containing alginate.

Locations

Country	Name	City	State
United Kingdom	The University of Nottingham	Nottingham	Nottinghamshire

Sponsors (2)

Lead Sponsor	Collaborator
University of Nottingham	Kaneka Corporation

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Small bowel water response to feeding	Area under the curve for small bowel water measured by MRI over four hours from baseline.	After four hours from baseline
Secondary	Gastric volume relative to baseline	Area under the curve for gastric volume relative to baseline, measured by MRI for four hours from baseline.	After four hours from baseline
Secondary	Mean post feeding gastric emptying rate	Mean gastric emptying rate calculated from MRI images of gastric volume obtained over four hours from baseline.	Over four hours from baseline.
Secondary	Superior mesenteric blood flow	Mean superior mesenteric blood flow calculated from measurements over four hours from baseline.	Over four hours from baseline.
Secondary	Incremental area under the curve for arterialised whole blood glucose	Incremental area under the curve for arterialised whole blood glucose will be calculated using samples collected at 10 minute intervals between baseline and four hours.	Over four hours post baseline
Secondary	Incremental area under the curve for insulin	Incremental area under the curve for insulin will be calculated using samples collected at 20 minute intervals between baseline and four hours.	Over four hours from baseline
Secondary	Incremental area under the curve for PYY (Peptide YY)	Incremental area under the curve for PYY will be calculated using samples collected at 20 minute intervals between baseline and four hours.	Over four hours from baseline
Secondary	Incremental area under the curve for Gastric Inhibitory Polypeptide	Incremental area under the curve for GIP will be calculated using samples collected at 20 minute intervals between baseline and four hours.	Over four hours from baseline
Secondary	Incremental area under the curve for Glucagon-like peptide 1 (GLP- 1)	Incremental area under the curve for GLP-1 will be calculated using samples collected at 20 minute intervals between baseline and four hours.	Over four hours from baseline
Secondary	Incremental area under the curve for Ghrelin	Incremental area under the curve for Ghrelin will be calculated using samples collected at 20 minute intervals between baseline and four hours.	Over four hours from baseline
Secondary	Incremental area under the curve for composite satiety score	Composite satiety score will be calculated using 100mm visual analogue score ratings of satiety, fullness, hunger and prospective food consumption collected every 30 minutes between baseline and four hours.	Over four hours from baseline
Secondary	Weight of consumption of a pasta meal four hours and thirty minutes after baseline.	Weight of pasta consumed from a bowl refilled prior to being empty until participants feel comfortably full.	Four hours and thirty minutes post baseline.
Secondary	Change in Faecal pH from baseline	The difference between faecal pH pre feeding and post feeding will be compared.	Comparison between sample obtained immediately before the enteral feeding day and samples obtained during the three days following the enteral feeding day.
Secondary	Faecal consistency	Rating of consistency of faecal sample will be compared with rating of consistency post enteral feeding day.	Comparison between sample obtained immediately before the enteral feeding day and samples obtained during the three days following the enteral feeding day.
Secondary	Incremental area under the curve for gastric symptom scores rated using visual analogue scores.	Incremental area under the curve for gastric symptoms will be calculated using 100mm visual analogue score ratings obtained every half hour between baseline and four hours.	Over four hours from baseline.